Matches in Nanopublications for { ?s ?p "[Megaloblastic anaemia 1 (MGA1, OMIM 261100) is a rare, autosomal recessive disorder characterized by juvenile megaloblastic anaemia, as well as neurological symptoms that may be the only manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_assertion description "[Megaloblastic anaemia 1 (MGA1, OMIM 261100) is a rare, autosomal recessive disorder characterized by juvenile megaloblastic anaemia, as well as neurological symptoms that may be the only manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_provenance.
- NP305188.RAxP1rpNdR-XAvHyeXIsyKepDCi3EpEMoBDx2O_uXAwxE130_assertion description "[Megaloblastic anaemia 1 (MGA1, OMIM 261100) is a rare, autosomal recessive disorder characterized by juvenile megaloblastic anaemia, as well as neurological symptoms that may be the only manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP305188.RAxP1rpNdR-XAvHyeXIsyKepDCi3EpEMoBDx2O_uXAwxE130_provenance.
- assertion description "[Megaloblastic anaemia 1 (MGA1, OMIM 261100) is a rare, autosomal recessive disorder characterized by juvenile megaloblastic anaemia, as well as neurological symptoms that may be the only manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Megaloblastic anaemia 1 (MGA1, OMIM 261100) is a rare, autosomal recessive disorder characterized by juvenile megaloblastic anaemia, as well as neurological symptoms that may be the only manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP247899.RAJa6OsXJYYRX7hqzM8zr0Nu0E2P7wkneqIgjcywqUwa0130_assertion description "[Megaloblastic anaemia 1 (MGA1, OMIM 261100) is a rare, autosomal recessive disorder characterized by juvenile megaloblastic anaemia, as well as neurological symptoms that may be the only manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP247899.RAJa6OsXJYYRX7hqzM8zr0Nu0E2P7wkneqIgjcywqUwa0130_provenance.
- NP788402.RAEP_WHLzqgwU9VsJ73bFb0SFpy_98BHIVg8Bb7FZXm7o130_assertion description "[Megaloblastic anaemia 1 (MGA1, OMIM 261100) is a rare, autosomal recessive disorder characterized by juvenile megaloblastic anaemia, as well as neurological symptoms that may be the only manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788402.RAEP_WHLzqgwU9VsJ73bFb0SFpy_98BHIVg8Bb7FZXm7o130_provenance.
- NP788378.RA3W3rCCR3lY76jexqWcOpj7OGeF0-Igi8aol9RnYsJT4130_assertion description "[Megaloblastic anaemia 1 (MGA1, OMIM 261100) is a rare, autosomal recessive disorder characterized by juvenile megaloblastic anaemia, as well as neurological symptoms that may be the only manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788378.RA3W3rCCR3lY76jexqWcOpj7OGeF0-Igi8aol9RnYsJT4130_provenance.
- NP247900.RA9OKZ5i5iyCefwugGebjM8_Jft5oTaHRo8jye9Xre2Zc130_assertion description "[Megaloblastic anaemia 1 (MGA1, OMIM 261100) is a rare, autosomal recessive disorder characterized by juvenile megaloblastic anaemia, as well as neurological symptoms that may be the only manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP247900.RA9OKZ5i5iyCefwugGebjM8_Jft5oTaHRo8jye9Xre2Zc130_provenance.